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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Alliance of Genome Resources
Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
| Source | Last Updated |
|---|---|
| Alliance of Genome Resources | July 29, 2024 |
| Disease ID ▼ | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0060770 | dextro-looped transposition of the great arteries | FB:FBgn0284408 | Drosophila melanogaster (fruit fly) | 45320 | trol | CG33950 |
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| DOID:0060759 | immunodeficiency with hyper IgM type 5 | HGNC:12572 | Homo sapiens (human) | 7374 | UNG |
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| DOID:0060759 | immunodeficiency with hyper IgM type 5 | SGD:S000004483 | Saccharomyces cerevisiae S288C | 854987 | UNG1 |
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| DOID:0060759 | immunodeficiency with hyper IgM type 5 | WB:WBGene00013241 | Caenorhabditis elegans | 176633 | ung-1 |
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| DOID:0060759 | immunodeficiency with hyper IgM type 5 | MGI:109352 | Mus musculus (house mouse) | 22256 | Ung |
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| DOID:0060740 | methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency | HGNC:7526 | Homo sapiens (human) | 4594 | MMUT |
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| DOID:0060732 | chromosome 9p deletion syndrome | HGNC:23399 | Homo sapiens (human) | 158326 | FREM1 |
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| DOID:0060728 | NGLY1-deficiency | HGNC:17646 | Homo sapiens (human) | 55768 | NGLY1 |
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| DOID:0060718 | autosomal recessive congenital ichthyosis 9 | HGNC:23752 | Homo sapiens (human) | 204219 | CERS3 |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | WB:WBGene00008431 | Caenorhabditis elegans | 174386 | piga-1 |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | ZFIN:ZDB-GENE-040426-1086 | Danio rerio (zebrafish) | 791759 | piga |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | MGI:99461 | Mus musculus (house mouse) | 18700 | Piga |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | HGNC:9491 | Homo sapiens (human) | 5652 | PRSS8 |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | Xenbase:XB-GENE-996765 | Xenopus tropicalis (tropical clawed frog) | 100158632 | piga |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | FB:FBgn0034270 | Drosophila melanogaster (fruit fly) | 37020 | PIG-A |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | RGD:1589723 | Rattus norvegicus (Norway rat) | 363464 | Piga |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | SGD:S000006096 | Saccharomyces cerevisiae S288C | 855928 | SPT14 |
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| DOID:0060710 | autosomal recessive congenital ichthyosis 2 | HGNC:430 | Homo sapiens (human) | 242 | ALOX12B |
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| DOID:0060704 | lymphoproliferative syndrome | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:0060680 | pigment dispersion syndrome | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:0060673 | Peters anomaly | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:0060669 | cerebral cavernous malformation | MGI:1206581 | Mus musculus (house mouse) | 18706 | Pik3ca |
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| DOID:0060669 | cerebral cavernous malformation | RGD:620916 | Rattus norvegicus (Norway rat) | 170911 | Pik3ca |
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| DOID:0060669 | cerebral cavernous malformation | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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